Label: UDDERBLEND SUPER - iodine liquid

  • NDC Code(s): 48106-1161-1, 48106-1161-2, 48106-1161-3, 48106-1161-4, view more
    48106-1161-5, 48106-1161-6
  • Packager: BouMatic, LLC
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 1, 2012

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    IODINE TEAT DIP CONCENTRATE

    Helps reduce the spread of organisms which may cause Mastitis

    NOT FOR HUMAN USE

    FOR EXTERNAL USE ONLY


    USE DIRECTIONS: Do not use in concentrated form. Must dilute prior to use.

    To obtain a 1% iodine solution and 5% emollient, add 1 gallon (4 L) of UDDERBLEND SUPER to 4 gallons (8L) of water and mix thoroughly.

    To obtain a 0.5% iodine solution and 2.5% emollient, add 1 gallon (4 L) of UDDERBLEND SUPER to 9 gallons (19 L) of water and mix thoroughly.


    PRE-DIPPING: Before milking, dip or spray entire teat with this product. Wipe teats dry after application using single-service towels to avoid contamination of milk.

    POST-DIPPING: After milking, spray or dip entire teat with this product. Allow to air dry.


    Note: If solution in cup becomes visibly dirty, replenish with a fresh mixture of this product. Do not return unused product to original container.

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  • CAUTION

    CAUTION

    KEEP OUT OF REACH OF CHILDREN
    NOT FOR HUMAN USE

    FIRST AID:
    If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses, if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed: Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do not induce vomiting. Contact a physician immediately. If breathing difficulty occurs: Move person to fresh air. Contact a physician immediately. If on skin: Take off contaminated clothing. Rinse skin with soap and water. If irritation develops and persists, contact a physician.
    Have the product container or label with you when going for treatment, calling a physician, the emergency number listed on this label or MSDS, or a poison control center.

    PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.

    STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.

    SEE MATERIAL SAFETY DATA SHEET

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  • PRINCIPAL DISPLAY PANEL



    Blank Label

    UDDERBLEND SUPER Label


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  • INGREDIENTS AND APPEARANCE
    UDDERBLEND SUPER 
    iodine liquid
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1161
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 450 g  in 10 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48106-1161-5 208 L in 1 DRUM
    2 NDC:48106-1161-6 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
    3 NDC:48106-1161-1 3.8 L in 1 DRUM
    4 NDC:48106-1161-2 18.9 L in 1 DRUM
    5 NDC:48106-1161-3 56.8 L in 1 DRUM
    6 NDC:48106-1161-4 114 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/01/2012
    Labeler - BouMatic, LLC (124727400)
    Registrant - BouMatic, LLC (124727400)
    Establishment
    Name Address ID/FEI Business Operations
    BouMatic, LLC 124727400 api manufacture, manufacture
    Establishment
    Name Address ID/FEI Business Operations
    Knapp Manufacturing 063012827 api manufacture, manufacture
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